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	601.	Dejerine-Sottas syndrome associated with point mutation in the peripheral myelin protein 22 (PMP22) gene. [electronic resource] by Roa, B B Dyck, P J Marks, H G Chance, P F Lupski, J R Producer: 19940204 In: Nature genetics vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	602.	Dejerine-Sottas disease with sensorineural hearing loss, nystagmus, and peripheral facial nerve weakness: de novo dominant point mutation of the PMP22 gene. [electronic resource] by Ionasescu, V V Searby, C Greenberg, S A Producer: 19970326 In: Journal of medical genetics vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	603.	Infantile axonal neuropathy in two siblings. [electronic resource] by Quinlivan, R M Robb, S A Hall, S M Honavar, M Hughes, R A Dubowitz, V Producer: 19941101 In: Neuromuscular disorders : NMD vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	604.	[Measuring vibration sense in childhood. Normal values and initial experiences in polyneuropathies]. [electronic resource] by Meister, C Molinari, L Thun-Hohenstein, L Boltshauser, E Producer: 19930809 In: Monatsschrift Kinderheilkunde : Organ der Deutschen Gesellschaft fur Kinderheilkunde vol. 141 Availability: No items available. Save to lists Add to cart (remove)
	605.	Dejerine-Sottas disease and hereditary demyelinating polyneuropathy of infancy. [electronic resource] by Plante-Bordeneuve, Violaine Said, Gérard Producer: 20021213 In: Muscle & nerve vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	606.	[Pilar dysplasia: an early marker of giant axonal neuropathy]. [electronic resource] by Rybojad, M Moraillon, I Bonafé, J L Cambon, L Evrard, P Producer: 19990405 In: Annales de dermatologie et de venereologie vol. 125 Availability: No items available. Save to lists Add to cart (remove)
	607.	Hereditary neuropathy with liability to pressure palsies in a Turkish patient (HNPP): a rare cause of entrapment neuropathies in young adults. [electronic resource] by Celik, Yahya Kilinçer, Cumhur Hamamcioğlu, M Kemal Balci, Kemal Birgili, Bariş Cobanoğlu, Sebahattin Utku, Ufuk Producer: 20080715 In: Turkish neurosurgery vol. 18 Availability: No items available. Save to lists Add to cart (remove)
	608.	Inflammatory demyelinating neuropathies and neuropathies associated with monoclonal gammopathies: treatment update. [electronic resource] by Steck, Andreas J Czaplinski, Adam Renaud, Susanne Producer: 20090105 In: Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	609.	A Novel Variant in the HINT1 Gene in a Girl with Autosomal Recessive Axonal Neuropathy with Neuromyotonia: Thorough Neurological Examination Gives the Clue. [electronic resource] by Rauchenzauner, Markus Frühwirth, Martin Hecht, Martin Kofler, Markus Witsch-Baumgartner, Martina Fauth, Christine Producer: 20161215 In: Neuropediatrics vol. 47 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	610.	[Motor and sensory neuropathies with or without agenesis of the corpus callosum: a radiological study of 64 cases]. [electronic resource] by Mathieu, J Bédard, F Prévost, C Langevin, P Producer: 19900731 In: The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques vol. 17 Availability: No items available. Save to lists Add to cart (remove)
	611.	Hereditary motor and sensory neuropathy with calf muscle enlargement. [electronic resource] by Sakashita, Y Sakato, S Komai, K Takamori, M Producer: 19930128 In: Journal of the neurological sciences vol. 113 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	612.	MRI of peripheral nerves and pathology of sural nerves in hereditary motor and sensory neuropathy type III. [electronic resource] by Tachi, N Kozuka, N Ohya, K Chiba, S Naganuma, M Producer: 19951218 In: Neuroradiology vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	613.	Hypertrophic neuropathy: atypical appearances resulting from the combination of type I hereditary motor and sensory neuropathy and diabetes mellitus. [electronic resource] by Thomas, P K King, R H Bradley, J L Producer: 19971106 In: Neuropathology and applied neurobiology vol. 23 Availability: No items available. Save to lists Add to cart (remove)
	614.	Correlation between quantitative EMG and muscle MRI in patients with axonal neuropathy. [electronic resource] by Jonas, D Conrad, B Von Einsiedel, H G Bischoff, C Producer: 20000810 In: Muscle & nerve vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	615.	Hereditary motor and sensory neuropathy--Lom (HMSNL): refined genetic mapping in Romani (Gypsy) families from several European countries. [electronic resource] by Chandler, D Angelicheva, D Heather, L Gooding, R Gresham, D Yanakiev, P de Jonge, R Baas, F Dye, D Karagyozov, L Savov, A Blechschmidt, K Keats, B Thomas, P K King, R H Starr, A Nikolova, A Colomer, J Ishpekova, B Tournev, I Urtizberea, J A Merlini, L Butinar, D Chabrol, B Voit, T Baethmann, M Nedkova, V Corches, A Kalaydjieva, L Producer: 20001222 In: Neuromuscular disorders : NMD vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	616.	3rd workshop of the European CMT consortium: 54th ENMC International Workshop on genotype/phenotype correlations in Charcot-Marie-Tooth type 1 and hereditary neuropathy with liability to pressure palsies 28-30 November 1997, Naarden, The Netherlands. [electronic resource] Producer: 19990624 In: Neuromuscular disorders : NMD vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	617.	Autosomal dominant Charcot-Marie-Tooth disease type 1A and hereditary neuropathy with liability to pressure palsies: detection of the recombination in Slovene patients and exclusion of the potentially recessive Thr118Met PMP22 point mutation. [electronic resource] by Leonardis, L Zidar, J Ekici, A Peterlin, B Rautenstrauss, B Producer: 19990322 In: International journal of molecular medicine vol. 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	618.	Marked phenotypic variation in a family with a new myelin protein zero mutation. [electronic resource] by Szabo, A Züchner, S Siska, E Mechler, F Molnar, M J Producer: 20060207 In: Neuromuscular disorders : NMD vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	619.	Hereditary neuropathy with liability to pressure palsy: a brief review with a case report. [electronic resource] by Rana, Abdul Qayyum Masroor, Mohamed Sufian Producer: 20121101 In: The International journal of neuroscience vol. 122 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	620.	Pain in hereditary neuropathy with liability to pressure palsy: an association with fibromyalgia syndrome? [electronic resource] by Yilmaz, Ugur Bird, Thomas T Carter, Gregory T Wang, Leo H Weiss, Michael D Producer: 20150421 In: Muscle & nerve vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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